Cornelia Damsky, Inc.

Cornelia Damsky, Inc. — FDA 510(k) Submissions

Cornelia Damsky, Inc. has submitted 4 FDA 510(k) premarket notifications since 1985, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powered Laser Surgical Instrument, Gauze/sponge, Internal, Strip, Adhesive, Closure, Skin . Use the specialty filter in the sidebar to narrow results.